7,519 variants MyGeneLog™ checks for — each with its own plain-language page and cited source. New findings are collected from the public GWAS Catalog every twenty minutes.
AGXT · rs6748734
See detailed info → Standard on its ownSLC6A13 · rs11062102
See detailed info → Standard on its ownSLC6A19 · rs11133665
See detailed info → SensitivePMVK · rs3766920
See detailed info → SensitiveQKI · rs6941513
See detailed info → Standard on its ownAHR · rs2892838
See detailed info → StandardCYP2A6 · rs184589612
See detailed info → StandardCYP2A6 · rs66500423
See detailed info → Standard on its ownARID3B · rs2470893
See detailed info → Standard on its ownAHR · rs10275488
See detailed info → Standard on its ownARID3B · rs35107470
See detailed info → Standard on its ownARID3B · rs12909047
See detailed info → StandardNCAM1 · rs17115310
See detailed info → Standard on its ownIRS1 · rs7578326
See detailed info → Standard on its ownNYAP2 · rs13422522
See detailed info → StandardHIVEP3 · rs12563071
See detailed info → StandardSLIT3 · rs2163761
See detailed info → StandardCPNE8 · rs826838
See detailed info → StandardCD46 · rs11118555
See detailed info → StandardSULT1C2 · rs17770672
See detailed info →Showing 20 of 7519 · page 223 of 376
One specific position in the genome (an rsID), explained in plain language with what published research has found it linked to, and how strong that link actually is.
The public GWAS Catalog, checked every twenty minutes, plus variants added manually after research review. Every one passes the same quality gate before publishing.
No. Listing reflects an association from published research, not a diagnosis or a cause. Most common variants shift probability modestly rather than determining an outcome.
Yes — the search box above matches gene symbols and rsIDs as well as trait names.